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Tetrahydrofuran → N-Methyl-p-(1-adamantyloxy)aniline

HRID 2050208
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HRID 2050208 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].C1COCC1.[CH:12]([NH:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][C:22]23[CH2:31][CH:26]4[CH2:27][CH:28]([CH2:30][CH:24]([CH2:25]4)[CH2:23]2)[CH2:29]3)=[CH:17][CH:16]=1)=O.[OH-].[Na+]>O>[CH3:12][NH:14][C:15]1[CH:16]=[CH:17][C:18]([O:21][C:22]23[CH2:31][CH:26]4[CH2:25][CH:24]([CH2:30][CH:28]([CH2:27]4)[CH2:29]2)[CH2:23]3)=[CH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8028Tetrahydrofuran2회HCID 14798Sodium HydroxideHCID 12510309N-Formyl-p-(1-adamantyloxy)anilineHCID 21226445Aluminium lithium hydride

생성물 1

HCID 12510299N-Methyl-p-(1-adamantyloxy)aniline

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

To a stirred suspension of 1.30 g. LiAlH4 in 20 ml. THF there was added 9.17 g. (0.034 mole) of N-formyl-p-(1-adamantyloxy)aniline in 200 ml. THF. Following 8 hours heating at reflux the mixture was cooled in ice and treated in turn with 1.3 ml. each of H2O and 15% NaOH and 4.9 ml. H2O. The inorganic gel was removed on a filter and the filtrate taken to dryness. The residue was recrystallized from Me2CO:SSB to give 5.96 g. (79%) of amine, N-methyl-p(1-adamantyloxy)aniline m.p. 134°-136°.

후처리

  1. additionTo a stirred suspension of 1.30 g
  2. temperatureheating
  3. temperatureat reflux the mixture
  4. temperaturewas cooled in ice
  5. additiontreated in turn with 1.3 ml
  6. customThe inorganic gel was removed on
  7. filtrationa filter
  8. customThe residue was recrystallized from Me2CO
  9. customSSB to give 5.96 g

출처 및 근거

ORD 기록
ord-878f01167a6a4ea79a551950c104e235
출처 데이터셋
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04200588

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